AEcelerate
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Meet the team building the evidence layer for clinical research and the offices where the work happens.

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Who We Are
TeamFounders, advisors, cliniciansCorporateMission, vision, and principlesOfficesChicago · Wilmington · Greensboro · London ON
Evidence & Knowledge
PublicationsPeer-reviewed work by our teamResourcesRegulatory references & literatureResearchIndia immersion & field researchPatentUSPTO filing, patent pendingConferencesExhibits & events, GHE 2026 Riyadh

A governed clinical-data foundation, an AI reasoning layer, and a human-in-the-loop review surface, built to meet trial deadlines.

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The ShiftWhy the model is changingStakeholdersProviders · CROs · SponsorsIntegrationsEpic, OpenFDA, ClinicalTrials.govVaultSecure clinical-data foundationPulseAI reasoning and AE detectionNavigatorHuman-in-the-loop reviewOur ProductsThe three systems of AEcelerate

Modular solutions for EHR and EDC connectors, survival outcomes, clinical training, analytics, and medical AI fine-tuning.

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EHR ConnectorsLive FHIR-based ingestionEDC ConnectorsBidirectional EDC syncSurvival OutcomesEndpoint analysisClinical SkillsTraining and assessmentHealth AnalyticsCohort and population insightsMed AI FinetuneDomain-tuned clinical models

AI agents that serve both sides of the visit: how patients reach care and how clinicians run it.

Open Agent Clinic
Patient Engagement & Access
Health OutreachIdentify and reach candidatesAccess OptimizationEligibility and coverageDigital Intake & TriageSelf-serve intakeVisit ReadinessPre-visit preparationLongitudinal CareContinuous monitoringCare Continuity & Follow-UpPost-visit loop closureAdherence & MonitoringProtocol compliance
Clinical Workflow Intelligence
Pre-Visit IntelligenceBrief the clinicianAI Documentation & Visit CopilotNote drafting in real timeCare PlanningPlan-of-care generationReferral CoordinationClosed-loop referrals

Operations across the United States, Canada, the Gulf, and Latin America; supporting sponsors and providers locally.

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USAChicago · Wilmington · GreensboroCanadaLondon, OntarioThe GulfGCC clinical operationsLatin AmericaLATAM partner network
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Resources

A reference shelf for clinical research teams.

The frameworks, registries, and literature our field works from; curated in one place so your team can find the governing document or the supporting evidence without the search.

Curated and verified by the AEcelerate team.

Regulatory & Compliance

The rules every study answers to.

Statutes, guidelines, and reporting frameworks that define how adverse events are documented and how trials stay compliant.

Code of Federal Regulations (Title 21)U.S. Government; eCFRThe codified body of FDA regulations governing drugs, devices, and biologics; the legal backbone for investigational studies, electronic records, and IRB oversight in U.S. clinical research.NCI Guidelines for Investigators: Adverse Event Reporting RequirementsNational Cancer Institute; CTEPWhat investigators on NCI-sponsored trials must report, on what timeline, and through which channels; the operating manual for AE expectations at participating sites.Good Clinical Practice GuidelinesU.S. Food and Drug AdministrationThe FDA's consolidated GCP reference; the international standard for designing, conducting, recording, and reporting trials so that data are credible and participant rights are protected.OHRP Guidance on Adverse Event Reporting (45 CFR 46)U.S. Government; eCFRThe Federal Policy for the Protection of Human Subjects; defines unanticipated-problem reporting duties and the IRB framework every U.S. research site operates under.
Registries & Safety Tools

Where trials are found and safety is tracked.

Public registries and NCI portals for locating studies and standardizing adverse-event monitoring.

ClinicalTrials.govNational Library of MedicineThe global registry of clinical studies; search by condition, intervention, location, or sponsor to find trials, review results, and track regulatory postings.CTEP Adverse Event Reporting SystemNational Cancer InstituteThe NCI's online portal for reporting and tracking adverse events in NCI-sponsored trials; the infrastructure behind standardized safety monitoring at participating institutions.Safety Profiler for Adverse Events (CTCAE)National Cancer InstituteA web tool built on the NCI standardized terminology for classifying and grading adverse events; consistency in severity language across studies and institutions.
Literature & Insights

Evidence and analysis on AI in research.

Peer-reviewed databases, oncology AI platforms, editorial analysis, and policy frameworks for responsible clinical AI.

PubMed / PMCNational Library of MedicineThe primary academic database for peer-reviewed literature on AI in clinical research; clinical-validation studies, implementation frameworks, and safety-reporting evidence.ASCO AIAmerican Society of Clinical OncologyASCO's platform equipping oncology professionals with tools, research, and guidelines for ethical, informed AI-supported decisions in cancer care.Cancer WorldCancer WorldEditorial coverage of AI-supported clinical decision-making in oncology; analysis of emerging tools and frameworks from organizations such as ASCO.Blueprint for an AI Bill of RightsThe White House; govinfoThe White House framework for responsible AI development; five principles spanning safety, equity, privacy, and human oversight that map directly onto clinical AI governance.
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Put these references to work in your workflow.

AEcelerate connects clinical documentation to governed, review-ready evidence; the regulatory clarity this shelf describes, implemented in the platform your team runs trials on.

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